Canonical Allele Identifier: PA2828912534
Gene: POR HGNC NCBI

Linked Data

ClinVar Variation Id: 16903
ClinVar RCV Id: RCV000018402 RCV001553652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369586.2:p.Cys566Tyr
CA257655
NM_001382657.2:c.1697G>A